Laboratorios Rovi
Pharmaceutical formulations, generic medicines and healthcare products.
Laboratorios Rovi manufactures pharmaceutical formulations, generic medicines and healthcare products from its Madrid operations. The company supplies pharmacy channels, hospital buyers, healthcare distributors or export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Madrid, Spain
- Founded
- 1946
- Website
- rovi.es
- Categories
- Medical & Healthcare Supplies, Supplements & Wellness
- Markets
- Spain, United States, Germany, France
Verified facts
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-09 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- vat-valid (green), checked 2026-08-09 VIES
- public-contract-awarded (green), checked 2026-05-13 TED (Tenders Electronic Daily), EU public procurement award notices Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
- export-registered (green), checked 2026-08-09 EU EORI validation (European Commission)
- public-subsidy-received (green), checked 2026-08-16 BDNS, Base de Datos Nacional de Subvenciones (Ministerio de Hacienda)
Profiles
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)